A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657333



Internal ID15047299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30053822..30154927hg38UCSC Ensembl
Innerchr9:30053820..30154925hg19UCSC Ensembl
Innerchr9:30043820..30144925hg18UCSC Ensembl
Innerchr9:30043820..30144925hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38101106
hg19101106
hg18101106
hg17101106
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657333
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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